{"title":"阳极差分脉冲伏安法测定片剂剂型中的多潘立酮","authors":"Tarek Wahdan, Nadia Abd El-Ghany","doi":"10.1016/j.farmac.2005.07.001","DOIUrl":null,"url":null,"abstract":"<div><p><span>A differential pulse voltammetric method was described for the determination of domperidone. The method was based on the anodic oxidation of domperidone on a glassy carbon electrode at +0.64 V vs. SCE in Britton–Robinson buffer solution of pH 2.3. The reversibility of the oxidation was tested by cyclic voltammetry; the electrode process is irreversible and diffusion–adsorption controlled. Calibrations are linear over the range 1.0</span> <!-->×<!--> <!-->10<sup>–6</sup>–2.0<!--> <!-->×<!--> <!-->10<sup>–5</sup> M of domperidone with a detection limit of 4.0<!--> <!-->×<!--> <!-->10<sup>–7</sup> M. The method was applied, without any interference from the excipients, to the determination of the drug in a tablet dosage form.</p></div>","PeriodicalId":77128,"journal":{"name":"Farmaco (Societa chimica italiana : 1989)","volume":"60 10","pages":"Pages 830-833"},"PeriodicalIF":0.0000,"publicationDate":"2005-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.farmac.2005.07.001","citationCount":"33","resultStr":"{\"title\":\"“Determination of domperidone in tablet dosage form by anodic differential pulse voltammetry”\",\"authors\":\"Tarek Wahdan, Nadia Abd El-Ghany\",\"doi\":\"10.1016/j.farmac.2005.07.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>A differential pulse voltammetric method was described for the determination of domperidone. The method was based on the anodic oxidation of domperidone on a glassy carbon electrode at +0.64 V vs. SCE in Britton–Robinson buffer solution of pH 2.3. The reversibility of the oxidation was tested by cyclic voltammetry; the electrode process is irreversible and diffusion–adsorption controlled. Calibrations are linear over the range 1.0</span> <!-->×<!--> <!-->10<sup>–6</sup>–2.0<!--> <!-->×<!--> <!-->10<sup>–5</sup> M of domperidone with a detection limit of 4.0<!--> <!-->×<!--> <!-->10<sup>–7</sup> M. The method was applied, without any interference from the excipients, to the determination of the drug in a tablet dosage form.</p></div>\",\"PeriodicalId\":77128,\"journal\":{\"name\":\"Farmaco (Societa chimica italiana : 1989)\",\"volume\":\"60 10\",\"pages\":\"Pages 830-833\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.farmac.2005.07.001\",\"citationCount\":\"33\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Farmaco (Societa chimica italiana : 1989)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0014827X05001539\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Farmaco (Societa chimica italiana : 1989)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014827X05001539","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 33
摘要
采用差分脉冲伏安法测定多潘立酮的含量。该方法是在pH为2.3的briton - robinson缓冲溶液中,用+0.64 V vs. SCE在玻碳电极上阳极氧化多潘立酮。用循环伏安法测定了氧化的可逆性;电极过程不可逆,扩散吸附可控。在多潘立酮浓度1.0 × 10 - 6 ~ 2.0 × 10-5 μ M范围内均呈线性,检出限为4.0 × 10-7 μ M。该方法在不受辅料干扰的情况下,可用于片剂型多潘立酮的测定。
“Determination of domperidone in tablet dosage form by anodic differential pulse voltammetry”
A differential pulse voltammetric method was described for the determination of domperidone. The method was based on the anodic oxidation of domperidone on a glassy carbon electrode at +0.64 V vs. SCE in Britton–Robinson buffer solution of pH 2.3. The reversibility of the oxidation was tested by cyclic voltammetry; the electrode process is irreversible and diffusion–adsorption controlled. Calibrations are linear over the range 1.0 × 10–6–2.0 × 10–5 M of domperidone with a detection limit of 4.0 × 10–7 M. The method was applied, without any interference from the excipients, to the determination of the drug in a tablet dosage form.